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FDA 510(k)

SFC VERTEBRAL BODY REPLACEMENT

K-Number: K110153 · 2011-10-12

ApplicantKonigsee Implantate GmbH
Decision Date2011-10-12
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SFC VERTEBRAL BODY REPLACEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Konigsee Implantate GmbH. It received FDA 510(k) clearance on 2011-10-12 under 510(k) number K110153. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SFC VERTEBRAL BODY REPLACEMENT?

SFC VERTEBRAL BODY REPLACEMENT is a medical device that received FDA 510(k) clearance on 2011-10-12. The listed applicant is Konigsee Implantate GmbH. The 510(k) number is K110153.

When did SFC VERTEBRAL BODY REPLACEMENT receive FDA 510(k) clearance?

SFC VERTEBRAL BODY REPLACEMENT received FDA 510(k) clearance on 2011-10-12, under 510(k) number K110153.

Who is the listed applicant for SFC VERTEBRAL BODY REPLACEMENT?

The FDA 510(k) record lists Konigsee Implantate GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SFC VERTEBRAL BODY REPLACEMENT?

The FDA product code for SFC VERTEBRAL BODY REPLACEMENT is MQP.

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Related Devices (Code: MQP)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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